FDA Adverse Event Injury Summary report: N

G7 PPS LTD ACET SHELL 50D

MDR report key: 10763581 · Received October 30, 2020

Report

Report Number
0001825034-2020-03968
Event Type
Injury
Date Received
October 30, 2020
Date of Event
September 9, 2020
Report Date
October 30, 2020
Manufacturer
ZIMMER BIOMET, INC.
Product Code
PBI
PMA / PMN Number
K121874
Removal / Correction Number
NI
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
OR, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

(B)(4). CONCOMITANT MEDICAL PRODUCTS: 30103604- G7 VIT E NEUTRAL LNR 36MM D- 64797263. 00877503602- BIOLOX® DELTA, CERAMIC FEMORAL HEAD, M, ø 36/0, TAPER 12/14- 2993410. 0106010003- AVENIR® MüLLER, STEM, STANDARD, UNCEMENTED, HA, 3, TAPER 12/14- 2966718. PROCEDURAL RELATED COMPLICATIONS ARE INFLUENCED BY THE TYPE OF SURGERY, PATIENTS PRE-EXISTING COMORBID STATE, AND PERIOPERATIVE MANAGEMENT. FACILITIES HAVE DISCHARGE CRITERIA THAT PATIENTS MUST MEET POST-SURGICAL PROCEDURE. IF THE DISCHARGE CRITERIA ARE NOT MET, THEN THE PATIENT WILL BE KEPT UNTIL THEY ARE STABLE FOR DISCHARGE, AND FOR THEIR SAFETY. THE DELAYED/PROLONGED HOSPITALIZATION IS NOT ABNORMAL, AS SIDE EFFECTS FROM ANESTHESIA ARE COMMON AND TYPICALLY RESOLVE WITHIN 24-48 HOURS. ANEMIA IS A CONDITION THAT DEVELOPS WHEN YOUR BLOOD IS DEFICIENT IN RED BLOOD CELLS (HEMOGLOBIN), WHICH LIMITS THE HEMOGLOBIN'S ABILITY TO CARRY ENOUGH OXYGEN THROUGHOUT THE BODY'S SYSTEM. WITH THE LACK OF OXYGEN, THE PATIENT CAN EXPERIENCE, LIGHT HEADEDNESS, WEAKNESS, FATIGUE, FAINTING, DIZZINESS, ELEVATED HEART RATE. ANEMIA CAN BE ASSOCIATED WITH DIFFERENT MEDICAL CONDITIONS OR CAN BE DIRECTLY RELATED TO BLOOD LOSS DURING A TRAUMA, SURGICAL PROCEDURE OR SURGICAL COMPLICATION. ANEMIA DEPENDING ON THE CAUSE CAN BE MONITORED AND TREATED MINIMALLY OR IF HEMOGLOBIN IS SIGNIFICANTLY LOW, IT COULD BE INDICATED THAT MEDICAL INTERVENTION IS NECESSARY TO TREAT, I.E. ADMINISTERING BLOOD OR OTHER MEDICAL INTERVENTIONS. AS POSTOPERATIVE DEVELOPMENT OF ANEMIA DEVELOPS WITH NO OTHER IDENTIFIED CAUSE, THIS SIGNIFIES A POSTOPERATIVE PROCEDURE-RELATED COMPLICATION. IF ANY FURTHER INFORMATION IS FOUND WHICH WOULD CHANGE OR ALTER ANY CONCLUSIONS OR INFORMATION, A SUPPLEMENTAL WILL BE FILED ACCORDINGLY. ZIMMER BIOMET WILL CONTINUE TO MONITOR FOR TRENDS.

Description of Event or Problem · 1

IT WAS REPORTED PATIENT EXPERIENCED POST-OPERATIVE ANEMIA AND HYPOTENSION REQUIRING MEDICAL INTERVENTION AND PROLONGED HOSPITALIZATION 2 DAYS¿ POST IMPLANTATION. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE AT THIS TIME.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1231571 G7 PPS LTD ACET SHELL 50D PROSTHESIS, HIP PBI ZIMMER BIOMET, INC. N/A 6727744

Patients

Seq Age Sex Outcome Treatment
1 Hospitalization| R